Evidence of the radioactive fallout in the center of Asia (Russia) following the Fukushima Nuclear Accident

It was recently reported that radioactive fallout due to the Fukushima Nuclear Accident was detected in environmental samples collected in the USA and Greece, which are very far away from Japan. In April-May 2011, fallout radionuclides (¹³⁴Cs, ¹³⁷Cs, ¹³¹I) released in the Fukushima Nuclear Accident were detected in environmental samples at the city of Krasnoyarsk (Russia), situated in the center of Asia. Similar maximum levels of ¹³¹I and ¹³⁷Cs/¹³⁴Cs and ¹³¹I/¹³⁷Cs ratios in water samples collected in Russia and Greece suggest the high-velocity movement of the radioactive contamination from the Fukushima Nuclear Accident and the global effects of this accident, similar to those caused by the Chernobyl accident.     

Anthropogenic radionuclides in sediment in the Japan Sea: distribution and transport processes of particulate radionuclides

Distributions of anthropogenic radionuclides (⁹⁰Sr, ¹³⁷Cs and ^239+240Pu) in seabed sediment in the Japan Sea were collected during the period 1998–2002. Concentration of ⁹⁰Sr, ¹³⁷Cs and ^239+240Pu in seabed sediment was 0.07–1.6 Bq kg⁻¹, 0.4–9.1 Bq kg⁻¹ and 0.002–1.9 Bq kg⁻¹, respectively. In the northern basin of the sea (Japan Basin), ^239+240Pu/¹³⁷Cs ratios in seabed sediment were higher and their variation was smaller compared to that in the southeastern regions of the sea. The higher ^239+240Pu/¹³⁷Cs ratios throughout the Japan Basin were considered to reflect production of Pu-enriched particles in the surface layer and substantial sinking of particulate materials in this region. In the southern regions of the Japan Sea (<38°N), both inventories and ^239+240Pu/¹³⁷Cs ratios in sediment were larger than those in the other regions. In the southern Japan Sea, observations suggested that supply of particulate radionuclides by the Tsushima Warm Current mainly enhanced accumulation of the radionuclides in this region.     

Global and local cancer risks after the Fukushima Nuclear Power Plant accident as seen from Chernobyl: A modeling study for radiocaesium (134Cs & 137Cs)

The accident at the Fukushima Daiichi Nuclear Power Plant (NPP) in Japan resulted in the release of a large number of fission products that were transported worldwide. We study the effects of two of the most dangerous radionuclides emitted, ¹³⁷Cs (half-life: 30.2 years) and ¹³⁴Cs (half-life: 2.06 years), which were transported across the world constituting the global fallout (together with iodine isotopes and noble gasses) after nuclear releases. The main purpose is to provide preliminary cancer risk estimates after the Fukushima NPP accident, in terms of excess lifetime incident and death risks, prior to epidemiology, and compare them with those occurred after the Chernobyl accident. Moreover, cancer risks are presented for the local population in the form of high-resolution risk maps for 3 population classes and for both sexes. The atmospheric transport model LMDZORINCA was used to simulate the global dispersion of radiocaesium after the accident. Air and ground activity concentrations have been incorporated with monitoring data as input to the LNT-model (Linear Non-Threshold) frequently used in risk assessments of all solid cancers. Cancer risks were estimated to be small for the global population in regions outside Japan. Women are more sensitive to radiation than men, although the largest risks were recorded for infants; the risk is not depended on the sex at the age-at-exposure. Radiation risks from Fukushima were more enhanced near the plant, while the evacuation measures were crucial for its reduction. According to our estimations, 730–1700 excess cancer incidents are expected of which around 65% may be fatal, which are very close to what has been already published (see references therein). Finally, we applied the same calculations using the DDREF (Dose and Dose Rate Effectiveness Factor), which is recommended by the ICRP, UNSCEAR and EPA as an alternative reduction factor instead of using a threshold value (which is still unknown). Excess lifetime cancer incidents were estimated to be between 360 and 850, whereas 220–520 of them will be fatal. Nevertheless, these numbers are expected to be even smaller, as the response of the Japanese official authorities to the accident was rapid. The projected cancer incidents are much lower than the casualties occurred from the earthquake itself (> 20,000) and also smaller than the accident of Chernobyl.     

Urban dose rates at Gävle, Göteborg and Lund

Besides gamma rays from ¹³⁷Cs emanating from the Chernobyl accident, gamma rays from natural radionuclides are a dominant source of radiation exposure to the public. Since people spend much more time indoors than outdoors the radiation dose obtained inside dwellings contributes greatly to individual and collective doses. Dose rate measurements were made at 20 locations within the city of Göteborg and at further 22 reference sites within a radius of 100 km. Measurements were also made at Gävle and Lund. The dose rates were measured with RNI intensimeters, TLD (LiF) meters and in in situ measurements using an HPGe. The ground cover was grass, asphalt, concrete slates or paving-stones. The dose rates varied between 0.05 and 0.25 μSv/h. Also performed in different ways, measurements made inside and outside buildings at both Göteborg and Gävle showed inside dose rates higher than outside dose rates.     

Fukushima fallout in Northwest German environmental media

Traces of short- and long-lived fallout isotopes (¹³¹I, ¹³⁴Cs and ¹³⁷Cs) were found in environmental samples collected in Northwest Germany (rain water, river sediment, soil, grass and cow milk) from March to May 2011, following the radioactivity releases after the nuclear accident in Fukushima, Japan. The measured concentrations are consistent with reported concentrations in air, amount of rainfall and expected values applying simple radioecological models. The [¹³⁴Cs]/[¹³⁷Cs] ratio reported for air (about 1) allows for discrimination between “recent” and “old” ¹³⁷Cs. Expected ¹³⁶Cs values fell below the detection limits of the instrumentation, despite large sample masses and long counting times.     

The radiological impact of the Chernobyl debris compared with that from nuclear weapons fallout

Our basic knowledge of the radiological impact of fallout from nuclear accidents is based on the experience gained from the study of nuclear weapons fallout. Radioecologically, the most important radionuclides generated by the Chernobyl accident were ¹³⁷Cs, ¹³⁴Cs, ¹³¹I and, to a lesser degree, ⁹⁰Sr. These nuclides are well known from global fallout, although in different relative amounts to those observed in the Chernobyl debris. Another important difference between the fallout from Chernobyl and that from nuclear weapon tests is that their seasonal and geographical distributions were quite dissimilar. A number of examples show how these differences influenced transfer factors and thus population doses. Special emphasis is paid to the contamination of milk and cereal products.Furthermore, it is shown how the composition of the Chernobyl debris changed with distance from Chernobyl, due to the differences in volatility of the various radionuclides involved. Finally, the paper compares the dose equivalents received from unit releases (1 P Bq ¹³⁷Cs) of global fallout and of Chernobyl accident debris.     

Recent levels of radionuclides in lichens from southwest Poland with particular reference to 134Cs and 137Cs

Analyses of Umbilicaria species collected from southwest Poland in August 1986 have shown there to be significant increases in levels of various radionuclides since previous analyses based on fieldwork in 1978–1979. The composition and ratio of the various radionuclides, particularly in respect of ¹³⁴Cs and ¹³⁷Cs, exhibit a characteristics signature consistent with contamination derived from the accident at the Chernobyl nuclear reactor in April 1986. Intraspecific variation in levels of ¹³⁷Cs in Umbilicaria is related to such factors as location, altitude and, to a lesser degree, aspect; interspecific variation in levels is related to ecological requirements and geographical pattern, and hence the same factors, although morphological differences in thalli may be implicated.     

Technogenic pollution of soil and plant cover in southern Primorye

Evaluation of technogenic load on ecosystems of southern Primorye has shown that the soil contents of ⁹⁰Sr and ¹³⁷Cs vary within the ranges of 0.3–1.3 and 0.4–3.0 kBq/m², respectively; i.e., they do not exceed the level of background radioactivity that is considered normal at latitudes between 50° and 60° N. The presence of ¹³⁴Cs in the samples indicates a contribution from radionuclides discharged by the Fukushima nuclear accident. According to calculations, the additional ¹³⁷Cs input into the soils of the study area varies between 0.03 and 0.30 kBq/m². Soil analysis for heavy metals and trace elements has revealed an approximately twofold excess over safety norms (MACs) in the concentrations of technogenic Cu and Pb. For other elements, the excess is within the range of 8–32%.     

Arrival time and magnitude of airborne fission products from the Fukushima, Japan, reactor incident as measured in Seattle, WA, USA

We report results of air monitoring started due to the recent natural catastrophe on 11 March 2011 in Japan and the severe ensuing damage to the Fukushima Dai-ichi nuclear reactor complex. On 17-18 March 2011, we registered the first arrival of the airborne fission products ¹³¹I, ¹³²I, ¹³²Te, ¹³⁴Cs, and ¹³⁷Cs in Seattle, WA, USA, by identifying their characteristic gamma rays using a germanium detector. We measured the evolution of the activities over a period of 23 days at the end of which the activities had mostly fallen below our detection limit. The highest detected activity from radionuclides attached to particulate matter amounted to 4.4 ± 1.3 mBq m⁻³ of ¹³¹I on 19-20 March.     

Contamination of Austrian soil with caesium-137

Austria ranks among the countries that have been most strongly affected by the Chernobyl fallout. The mean contamination with 137Cs is 21.0 kBq/m2, of which 18.7 kBq/m2 is due to the Chernobyl accident, whereas global fallout contributes 2.3 kBq/m2. Maximum values of total 137Cs contamination are nearly 200 kBq/m2. Total deposition of Chernobyl 137Cs on Austrian territory is 1.6 PBq or a fraction of around 2% of the 137Cs released from the reactor. 2115 measurements were used to draw the Austrian "caesium map". The geographical pattern of fallout distribution shows regional differences of contamination as high as 1:100.     

Studies of 131I, 137Cs and 103Ru in milk,meat and vegetables in North East Scotland following the Chernobyl accident

Uptake and clearance of radionuclides in foodstuffs have been studied in the neighbourhood of Aberdeen in North East Scotland following the Chernobyl accident. The level of¹³¹ I in goats' milk was 100–200 Bq litre⁻¹ in early May and declined with an effective half-life of 4sd3 days, but that in cows' milk was only a few Bq litre⁻¹ as most cattle were kept indoors. ¹³⁷Cs and ¹⁰³Ru activities in broccoli declined with effective half-lives of 11 and 6 days respectectively, while ¹³⁷Cs in grass decresed with a half-life of 22 days, the reduction appearing to show a relationship to weekly rainfall. Studies of tissues from groups of lambs initially grazed on contaminated pasture and later (a) fed indoors on concentrates or (b) continuing to graze outdoors, showed the ¹³⁷Cs concentrations to decline with half-lives of (a) 17 days and (b) 25 days, while the half-lives describing the reduction in total ¹³⁷Cs activity were (a) 20 days and (b) 35 days.     

Weather-dependent change of cesium,strontium, barium and tellurium contamination deposited as aerosols on various cultures

Various types of plants (wheat, bean, lettuce, radish and grass) were contaminated by dry deposition of radioactive aerosols (¹³⁷Cs, ⁸⁵Sr, ¹³³Ba and ^123mTe) in order to supplement the radioecological data necessary for operational post-accidental codes. A few days after deposition, rainfalls were applied to these cultures to evaluate the influence of some characteristics of the rain on the contamination of the culture over time. On the other hand, for wheat and bean, the influence of the humidity condition of the foliage at the contamination time was considered. For a given plant species at a given vegetative stage, the four radionuclides were intercepted in an identical way. The interception varied from 30% for bean (young sprout) to 80% for lettuce (near maturity). The global transfer factor values were dependent on both the radionuclides and the plant species; nevertheless, a higher value was obtained for cesium, regardless of the plant and the rainfall (from 0.006 m² kg_fresh⁻¹ for wheat-grains – contaminated at the shooting stage – or for bean-pods – contaminated at the pre-flowering stage – to 0.1 m² kg_fresh⁻¹ for a whole lettuce). The analysis of the results allowed us on the one hand, to extract parameter values of the foliar transfer directly usable in operational codes, in particular those relating to barium and tellurium, unknown until then, and on the other hand, to lay the foundations of a future, more mechanistic model, taking into account the foliar processes in a finer way.     

Radioactive impact of Fukushima accident on the Iberian Peninsula: evolution and plume previous pathway

High activity concentrations of several man-made radionuclides (such as (131)I, (132)I, (132)Te, (134)Cs and (137)Cs) have been detected along the Iberian Peninsula from March 28th to April 7th 2011. The analysis of back-trajectories of air masses allowed us to demonstrate that the levels of manmade radionuclide activity concentrations in the southwest of the Iberian Peninsula come from the accident produced in the nuclear power plant of Fukushima. The pathway followed by the radioactive plume from Fukushima into Huelva (southwest of the Iberian Peninsula) was deduced through back-trajectories analysis, and this fact was also verified by the activity concentrations measured of those radionuclides reported in places crossed by this radioactive cloud. In fact, activity concentrations reported by E.P.A., and by IAEA, in several places of Japan, Pacific Ocean and United States of America are according to the expected ones from the air mass trajectory arriving at Huelva province.     

Transfer of Chernobyl-derived 134Cs, 137Cs, 131I and 103Ru from flowers to honey and pollen

The activity concentrations of ¹³⁷Cs, ¹³⁴Cs, ¹³¹I and ¹⁰³Ru were determined separately in honey and pollen samples collected from a single bee colony during several months after the deposition of Chernobyl fallout. The source of each honey and pollen sample was determined by pollen analysis. Although the activity concentrations in honey and pollen varied with time, the concentrations of ¹³⁷Cs and ¹³⁴Cs were, in general, higher in pollen than in honey. For ¹⁰³Ru and ¹³¹I, these differences were comparatively small. The mean ¹³¹ I/¹³⁷Cs and ¹⁰³Ru/¹³⁷Cs ratios were about one order of magnitude higher in honey than in pollen. The mean ¹³¹I/¹⁰³Ru ratio was about the same for honey and pollen. This observation, in the light of the corresponding nuclide ratios found in the deposition, suggests that ¹³⁷Cs, ¹³⁴Cs, ¹³¹I and ¹⁰³Ru were taken up by the plant leaves and transported to nectar and pollen. The higher activity concentrations of ¹³⁷Cs and ¹³⁴Cs in pollen, relative to honey, indicate that these radionuclides behave analogously to potassium, which is also found in higher quantities in pollen.     

Validation of the ICRP model for caesium intake by lactating mothers with Italian data after the Chernobyl fallout

In the aftermath of the Chernobyl nuclear power plant accident, a research group of the Italian National Institute of Health (Istituto Superiore di Sanità) carried out two research programmes on maternal milk. One concerned the transfer of caesium radionuclides from the diet to breast milk. In the other, the activity concentrations of ¹³⁷Cs were also determined in urine and placenta. The first study estimated the mothers’ average ¹³⁷Cs dietary intake, in the second study the intake was evaluated individually for each subject. In 2004, the International Commission on Radiological Protection published modified systemic biokinetic models which also account for transfer to breast milk. The model for caesium radionuclides was implemented and tested by the authors with the experimental data described above. A good agreement was obtained between measured data and model simulations of ¹³⁷Cs activity concentration in human milk. The model, however, tends to systematically overestimate ¹³⁷Cs activity concentration in urine, in which case the agreement is to be considered satisfactory in terms of order of magnitude.     

Fallout in the New York metropolitan area following the chernobyl accident

In the metropolitan New York area, maximum concentrations in air of radioactive aerosol and gaseous debris from the Chernobyl accident of April 1986 were much lower than those measured in Europe. The observed maxima were: for gaseous ¹³¹I, 23mBq m⁻³; for aerosol samples, 20mBq m⁻³ of ¹³¹I and 9·mBq m⁻³ of ¹³⁷Cs. The data suggest that little gas-to-particle transformation of iodine occurred during transport of the radioactive cloud from the Ukraine to New York. The ratios of ¹⁰³Ru and other refractories to ¹³⁷Cs were low in the first debris sampled, debris which probably was emitted from Chernobyl in late April during the early stages of the accident. In subsequent samples these ratios were higher, presumably because debris from the later, hotter stages of the fire had reached our sampling sites. A significant fraction (25–40%) of the deposition of ¹³¹I and ¹³⁷Cs into our samplers and on grass was by dry deposition. The total deposition of Chernobyl ¹³⁷Cs in the area was <1% of that already present in the soil from fallout from past nuclear weapon tests. The highest concentration of ¹³¹I measured in fresh milk was about 1.5 B1 liter⁻¹, <0.1% of the US action level. The dose to the thyroid of a six-month-old infant who had fresh milk as a sole food source would be about 70 μGy (7 mrad).     

The marine impact of caesium-134 and -137 from the Chernobyl reactor accident

¹³⁴Cs and ¹³⁷Cs from the Chernobyl reactor accident were detected in UK shoreline seawater very quickly after activity from the accident reached this country. Concentrations were highest in areas adjacent to those where deposition over land was highest, but they declined quickly and did not reach radiologically significant levels in terms of public radiation exposure. Subsequently, the distribution in seawater was investigated further afield. Radiocaesium attributable to the Chernobyl accident was found to be widespread: it was readily distinguished from other sources by having a different ¹³⁷Cs:¹³⁴Cs ratio (about 2:1). Its presence was especially noticeable in northern UK waters rather than those to the south; much of the North Sea has been surveyed as well as the Norwegian Sea. Evidence of Chernobyl radiocaesium was found as far north as 70°N and in many of these areas, including the northern North Sea, it overshadowed the effect of BNFL (British Nuclear Fuels plc) Sellafield discharges, previously the main source of these radionuclides.     

Radioiodine and radiocesium in Thessaloniki, Northern Greece due to the Fukushima nuclear accident

Radioiodine (¹³¹I) in air and rainwater as high as 497 μBq m⁻³ and 0.7 Bq L⁻¹, respectively, as well as ¹³⁷Cs and ¹³⁴Cs in air as high as 145 μBq m⁻³ and 126 μBq m⁻³, respectively were recorded in Thessaloniki, Northern Greece (40°38′N, 22°58′E) from March 24, 2011 through April 09, 2011, after a nuclear accident occurred at Fukushima, Japan (37°45′N, 140°28′E) on March 11, 2011.     

Occurrence and behaviour of radionuclides in the Moselle River-Part II: Distribution of radionuclides between aqueous phase and suspended matter

Most of the radionuclides released from nuclear power plants ( NPPs) into rivers are primarily adsorbed onto suspended matter. To describe this nuclide transfer, a model was used which takes the total suspended matter load as solid phase into account. The necessary partition factors of various radionuclides were determined in river water/suspended matter of the Moselle in laboratory investigations. By use of this model, a conservative estimate of the radionuclide concentration of the solid phase could be obtained which proved to be more realistic than the results based on the distribution law.Furthermore, the influence of grain-size on the specific activity of single fractions of a Moselle sediment was demonstrated using ¹³⁷Cs, ¹⁰⁶Ru and ¹⁴⁴Ce from the Chernobyl nuclear accident as tracers. The grain-size pattern is considered to be a main factor which may seriously distort the determination of distribution coefficients and concentration factors that are needed in applying the model based on the distribution law.     

Global transport rates of Cs and Pu originating from the Nagasaki A-bomb in 1945 as determined from analysis of Canadian Arctic ice cores

Recent advancements in analytical technology make it possible for artificial radionuclides released from nuclear explosions to be detected in Arctic ice core layers. The fission product, ¹³⁷Cs, and the unexpended fission material, ^239+240Pu, originating from the Nagasaki A-bomb of August 1945, were measured by collecting 10 ice cores on the Agassiz ice cap, Ellesmere Island, Canada. The deposition rates were 0·020 mBq cm^-2 for ¹³⁷Cs and 0·0016 mBq cm^-2 for ^239+240Pu, originating from Nagasaki. Assuming the radionuclides, excluding the amount fissioned from the explosion and deposi-ted as local fallout, are deposited evenly throughout the Northern Hemisphere, 67% of the expected amount of ¹³⁷Cs reached the Arctic while 1·1% of ^239+240Pu reached the Arctic. The results suggest that different transport mechanisms exist for various contaminants in the global transport system.